Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs659366
rs659366
Entrez Id: 7351
Gene Symbol: UCP2
UCP2
CUI: C0948089
Disease:
Acute Coronary Syndrome
0.010 GeneticVariation BEFREE In our study we analysed the association between LTL and five selected variants within three candidate genes (TERC rs12696304; TERF2IP rs3784929 and rs8053257; UCP2 rs659366 and rs622064), which are not only involved in telomere-length maintenance but also potentially associated with higher risk of acute coronary syndrome (ACS) in Czech women (505 cases and 642 controls). 26765095 2016